ClinVar Miner

Submissions for variant NM_001042492.3(NF1):c.5676dup (p.Leu1893fs)

dbSNP: rs1475358670
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Human Genetics, Inc, Center for Human Genetics, Inc RCV000660084 SCV000782060 pathogenic Neurofibromatosis, type 1 2016-11-01 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000660084 SCV002175621 pathogenic Neurofibromatosis, type 1 2021-05-03 criteria provided, single submitter clinical testing This sequence change creates a premature translational stop signal (p.Leu1872Thrfs*20) in the NF1 gene. It is expected to result in an absent or disrupted protein product. Loss-of-function variants in NF1 are known to be pathogenic (PMID: 10712197, 23913538). This variant is not present in population databases (ExAC no frequency). This variant has not been reported in the literature in individuals with NF1-related conditions. ClinVar contains an entry for this variant (Variation ID: 547666). For these reasons, this variant has been classified as Pathogenic.
Genome-Nilou Lab RCV000660084 SCV002560139 pathogenic Neurofibromatosis, type 1 2022-03-15 criteria provided, single submitter clinical testing

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